Abstract
A robust polymeric material constituted by chains of binuclear aqua ruthenium terpyridylphenanthroline complexes connected through benzene ring meta-positions, exhibiting an unusual two electrons and two protons PCET (proton-coupled electron transfer) process and enhanced oxygen evolution reaction (OER) activity, is described. The catalytic active [RuV[dbnd]O] species is generated at potentials more positive than +1.5 V (NHE) in the poly-[{Ru(H2O)(phen)}2(tpy2ph)] film, as confirmed by the rise of the ruthenyl (RuV[dbnd]O) stretching band at 810 cm−1 in the Raman spectrum, and the clear change to a higher activity regime as confirmed by EIS. Faradaic efficiency for OER as high as 39% was achieved at +1.8 V, indicating that poly-[{Ru(H2O)(phen)}2(tpy2ph)] is one of the most active ruthenium terpyridine complexes ever prepared. The synthesis and characterization of the monomeric binuclear [{RuCl(Clphen)}2(tpy2ph)]2+ and its respective [{Ru(H2O)(Clphen)}2(tpy2ph)]4+ aqua complex are also fully described.
Original language | English |
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Pages (from-to) | 18-26 |
Number of pages | 9 |
Journal | Electrochimica Acta |
Volume | 283 |
DOIs | |
State | Published - 1 Sep 2018 |
Externally published | Yes |
Keywords
- Binuclear catalyst
- Electrocatalysis
- High valence complex
- Modified electrodes
- Oxygen evolution reaction
- Ruthenium complex